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rs878855090

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855090(-;-)
Make rs878855090(-;AG)
Make rs878855090(AG;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position193142025
GeneCDC73
is asnp
is mentioned by
dbSNPrs878855090
ebirs878855090
HLIrs878855090
Exacrs878855090
Varsomers878855090
Maprs878855090
PheGenIrs878855090
hapmaprs878855090
1000 genomesrs878855090
hgdprs878855090
ensemblrs878855090
gopubmedrs878855090
geneviewrs878855090
scholarrs878855090
googlers878855090
pharmgkbrs878855090
gwascentralrs878855090
openSNPrs878855090
23andMers878855090
23andMe allrs878855090
SNP Nexus

SNPshotrs878855090
SNPdbers878855090
MSV3drs878855090
GWAS Ctlgrs878855090
Max Magnitude0
ClinVar
Risk rs878855090(AG;AG)
Alt rs878855090(AG;AG)
Reference rs878855090(;)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193111154_193111155dupAG
CLNSRC
CLNACC RCV000226610.1,